Allele Registry

Canonical Allele Identifier: PA2827786781

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000479372

ClinVar Variation:

420677

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340887.1:p.Pro1731Ser	CA16617281 NM_001353958.2:c.5191C>T